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Filtered Search Results
eMolecules 63721-14-2 | NH-bis(PEG3-OH) | Broadpharm | MFCD29912667 | 369.455 | C16H35NO8 | 96.000 | OCCOCCOCCOCCNCCOCCOCCOCCO | 1g | 311074464
NH-bis(PEG3-OH) | Broadpharm | 63721-14-2 | MFCD29912667 | 369.455 | C16H35NO8 | 96.000 | OCCOCCOCCOCCNCCOCCOCCOCCO | 1g | 311074464
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Medchemexpress LLC Thalidomide-NH-CBP/p300 ligand 2 | 2484739-21-9 | 98.55% | 922.03 | 50 MG
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Thalidomide-NH-CBP/p300 ligand 2 (P-007) is a PROTAC-based CBP and p300 degrader. It is for research use only and not sold to patients. This compound is extracted from patent WO2020173440 and targets Cereblon.
- PROTAC-based degrader
- Targets CBP and p300
- For research use only
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Medchemexpress LLC 2-Butenamide, N-[1,1'-biphenyl]-4-yl-2-cyano-3-hydroxy- | 1173715-42-8 | 99.9% | 278.31 g/mol | C17H14N2O2 | 5 MG
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hDHODH-IN-1 is a small-molecule inhibitor of human dihydroorotate dehydrogenase (hDHODH) with reported anti-inflammatory activity. It is supplied as a high-purity research reagent intended for in vitro and preclinical laboratory studies.
- Potent inhibitor of human dihydroorotate dehydrogenase (hDHODH).
- Demonstrated anti-inflammatory activity in biological assays.
- High purity: 99.90% (LCMS).
- Molecular formula C17H14N2O2 and molecular weight 278.31 g/mol.
- Supplied as a 5 mg pack for laboratory research use.
- Intended for research use only; not for human or clinical applications.
- Certificate of analysis available for quality verification.
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Medchemexpress LLC Raf265 (CHIR-265) | 927880-90-8 | MFCD16659061 | 99.8% | 518.41 g/mol | C24H16F6N6O | 25 MG
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RAF265 (CHIR-265) is a small-molecule, orally active RAF and VEGFR2 kinase inhibitor used in oncology research and preclinical studies.
- Potent RAF and VEGFR2 inhibitor for research applications.
- Orally active small molecule.
- Molecular formula C24H16F6N6O.
- Molecular weight 518.41 g/mol.
- Physical form: powder.
- Purity: 99.8%.
- Storage: powder -20°C (3 years) or 4°C (2 years).
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC N-[5-[[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-2-methylphenyl]propanamide | 2470424-39-4 | 99.7% | C20H21N7O | 10MG
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SGC-CK2-1 is a selective, cell-active ATP-competitive chemical probe for casein kinase 2 (CK2) used in research to investigate CK2 signaling and neurodegenerative disease-related pathways. It shows low-nanomolar potency in cellular assays and is suitable for mechanistic and cell-based studies.
- Low-nanomolar cellular potency against CK2 isoforms.
- High selectivity for CK2 over other kinases.
- Cell-permeable and active in cell-based assays.
- Suitable for mechanistic studies of CK2 signaling and neurodegeneration.
- Stable solid form with recommended cold storage for long-term retention.
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eMolecules 1213949-37-1 | (R)-3-(3-CHLOROPHENYL)-BETA-ALANINOL | AstaTech | MFCD07784066 | 185.650 | C9H12ClNO | 95.000 | N[C@H](CCO)c1cccc(Cl)c1 | 1g | 112525363
(R)-3-(3-CHLOROPHENYL)-BETA-ALANINOL | AstaTech | 1213949-37-1 | MFCD07784066 | 185.650 | C9H12ClNO | 95.000 | N[C@H](CCO)c1cccc(Cl)c1 | 1g | 112525363
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Medchemexpress LLC Upacicalcet sodium | 2052969-18-1 | 99.9% | 373.75 g/mol | C11H13ClN3NaO6S | 5 MG
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Upacicalcet sodium is a non-peptide calcimimetic that acts as a calcium-sensing receptor (CaSR) agonist and is used in preclinical research to reduce intact parathyroid hormone (iPTH) and serum calcium levels, with reported effects on vascular calcification and bone abnormalities in secondary hyperparathyroidism models.
- Potent CaSR agonist (reported EC50 = 10.8 nM).
- Reduces serum intact parathyroid hormone and lowers serum calcium.
- Shown to improve vascular calcification and bone disorder outcomes in preclinical models.
- Offered in multiple research quantities and as ready-to-use DMSO solutions.
- Suitable for studies of secondary hyperparathyroidism and chronic kidney disease-related bone effects.
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Medchemexpress LLC M-89 | 2363165-42-6 | 99.1% | 657.87 g/mol | C37H47N5O4S | 5 MG
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M-89 is a potent, selective menin-MLL interaction inhibitor supplied as a research compound for preclinical biochemical and cellular studies. It is used to disrupt the menin-MLL protein-protein interaction in epigenetic and leukemia research.
- Potent menin-MLL protein-protein interaction inhibitor (Kd 1.4 nM).
- High purity (99.1%) suitable for biochemical assays.
- Soluble in DMSO at approximately 7.35 mg/mL with ultrasonic assistance.
- Available in small research quantities for exploratory studies.
- Stable when stored as powder at low temperatures for long-term use.
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eMolecules 758679-97-9 | Medchem Express | CID-2858522 | 5mg | 446265893 | HY-15530 | MFCD20755108 | 465.638 | C28H39N3O3
Medchem Express | CID-2858522 | 5mg | 446265893 | HY-15530 | 758679-97-9 | MFCD20755108 | 465.638 | C28H39N3O3
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eMolecules 179075-88-8 | 1-BUTYL-3-METHYLIMIDAZOLIUM NITRATE | AstaTech | MFCD08457696 | 201.226 | C8H15N3O3 | 95.000 | [O-][N+]([O-])=O.CCCCn1cc[n+](C)c1 | 1g | 449723053
1-BUTYL-3-METHYLIMIDAZOLIUM NITRATE | AstaTech | 179075-88-8 | MFCD08457696 | 201.226 | C8H15N3O3 | 95.000 | [O-][N+]([O-])=O.CCCCn1cc[n+](C)c1 | 1g | 449723053
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Medchemexpress LLC HY-104021 10mg Medchemexpress, GSK840 CAS:2361146-30-5 Purity:>98%
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Medchemexpress, HY-104021 10mg GSK840 CAS:2361146-30-5 GSK840 (GSK'840) is a receptor-interacting protein kinase 3 (RIP3 or RIPK3) inhibitor, which binds RIP3 kinase domain with an IC50 of 0.9 nM, and inhibits kinase activity with an IC50 of 0.3 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-10194 10mg Medchemexpress, Sepantronium (bromide) CAS:781661-94-7 Purity:>98%
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Medchemexpress, HY-10194 10mg Sepantronium (bromide) CAS:781661-94-7 Sepantronium bromide (YM-155) is a survivin inhibitor with an IC50 of 0.54 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-F0003A 10mg Medchemexpress, NADPH (tetracyclohexanamine) CAS:100929-71-3 Purity:>98%
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Medchemexpress, HY-F0003A 10mg NADPH (tetracyclohexanamine) CAS:100929-71-3 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-103181 50mg Medchemexpress, N6-Cyclopentyladenosine CAS:41552-82-3 Purity:>98%
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Medchemexpress, HY-103181 50mg N6-Cyclopentyladenosine CAS:41552-82-3 N6-Cyclopentyladenosine (CPA) is a selective Adenosine A1 receptor agonist, with Ki values of 2.3 nM, 790 nM and 43 nM for human A1, A2A and A3 receptors, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 7803-88-5 | Medchem Express | 6-O-Methyl Guanosine | 50mg | 451965701 | HY-111648 | 297.271 | C11H15N5O5
Medchem Express | 6-O-Methyl Guanosine | 50mg | 451965701 | HY-111648 | 7803-88-5 | 297.271 | C11H15N5O5
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